FDAnews
www.fdanews.com/articles/72221-drug-development-meetings

Drug Development Meetings

May 12, 2005

Join FDAnews Thursday, May 19, for a 90-minute audioconference on "Preparing Successful eCTDs: Compliant Submissions the First Time, Every Time." Learn how to correctly prepare your electronic common technical documents to the FDA's expectations. On May 20, join FDAnews for "Voluntary No More -- California's New Mandatory Rules for Drug and Device Firms: Compliance and Marketing Strategies to Meet Your July 1 Deadline." Learn about the landmark legislation that is changing the rules for drugmakers and devicemakers in California, the key components for meeting the deadline, and how others are complying.

May 16-18: Clinical Data Management

Philadelphia, Pa.

(703) 276-0178

Peri

maria.simonetti@peri.org

www.peri.org

May 17-18: Improving Investigator and Site Management Using CTMS

Webcast

(609) 524-4100

ClinPhone

info@clinphone.com

www.clinphone.com

May 18-19: GLP Training

Philadelphia, Pa.

(443) 543-5530

SPI USA

seminars@usaspi.com

www.usaspi.com

May 18-19: Innovation Boot Camp

Newport Beach, Calif.

(714) 289-1233

Institute for Effective Innovation

info@innovationbootcamp.com

www.InnovationBootCamp.com

May 18-19: Parenteral Product Development

Malvern, Pa.

(610) 688-1708

The Center for Professional Innovation & Education

lcourville@cfpie.com

www.cfpie.com

May 18-20: Advanced Good Clinical Practices

Bethesda, Md.

(703) 276-0178

Peri

maria.simonetti@peri.org

www.peri.org

May 19: Preparing Successful eCTDs

Compliant Submissions the First Time, Every Time

Your Office

An audioconference

(703) 538-7600

FDAnews

www.fdanews.com/wbi/conferences/ectd.html (http://www.fdanews.com/wbi/conferences/ectd.html)

May 19-20: Risk-Based Approach to Computer Compliance Focusing on Clinical Trials

Phoenix, Ariz.

(919) 531-5369

SEC Associates and SAS

Dori.Pyles@SAS.com

http://support.sas.com/training/us/crs/bracc.html

May 20: Voluntary No More -- California's New Mandatory Rules for Drug and Device Firms

Compliance and Marketing Strategies to Meet Your July 1 Deadline

An audioconference

Your Office

(703) 538-7600

FDAnews

www.fdanews.com/wbi/conferences/californialaw.html (http://www.fdanews.com/wbi/conferences/californialaw.html)

May 23-25: 15th International Contracting and Negotiating Clinical Trials

Philadelphia, Pa.

(212) 967-0095

Strategic Research Institute

sgrodsky@srinstitute.com

www.srinstitute.com/cs317

May 23-25: IIR's Optimizing Preclinical Outsourcing

Boston, Mass.

(212) 661-3500

Institute for International Research

slee@iirusa.com

www.iirusa.com/preclinicaloutsourcing

May 24: Reduce Supply Chain Risks

How the FDA Expects You to Manage Outsourced Suppliers

An FDAnews audioconference With Martin Browning

Your Office

(703) 538-7600

FDAnews

www.fdanews.com/wbi/conferences/supplychain.html (http://www.fdanews.com/wbi/conferences/supplychain.html)

May 24-25: CHI's Third Annual R&D Strategies: Managing Risk to Increase Productivity

Philadelphia, Pa.

(617) 630-1300

Cambridge Healthtech Institute

chi@healthtech.com

http://www.worldpharmacongress.com/

May 24-25: Monitoring of Clinical Trials

Malvern, Pa.

(610) 688-1708

The Center for Professional Innovation & Education

info@cfpie.com

www.cfpie.com

May 24-26: CHI's World Pharmaceutical Congress

Philadelphia, Pa.

(617) 630-1300

Cambridge Healthtech Institute

chi@healthtech.com

www.healthtech.com

May 25: Deviation Investigation Report Writing

Somerset, N.J.

(801) 685-7717 x306

McCulley/Cuppan

jgregg@mcculley-cuppan.com

www.mcculley-cuppan.com

May 25: FDA's New Risk Management Guidances

Roadmaps and RiskMAPs for Improving Drug Safety

An audioconference

Your Office

(703) 538-7600

FDAnews

www.fdanews.com/wbi/conferences/riskmaps.html (http://www.fdanews.com/wbi/conferences/riskmaps.html)